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914096

Sigma-Aldrich

1,3-Bis(2,6-di(3-pentyl)phenyl)imidazolium chloride

≥95%

别名:

IPent-HCl

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About This Item

经验公式（希尔记法）:
C35H53ClN2
CAS号:
1157867-61-2
分子量:
537.26
MDL號碼:
MFCD27978383
分類程式碼代碼:
12352005
NACRES:
NA.22

品質等級

100

化驗

≥95%

形狀

powder

mp

362-364 °C

SMILES 字串

[Cl-].[n+]2(c[n](cc2)c3c(cccc3C(CC)CC)C(CC)CC)c1c(cccc1C(CC)CC)C(CC)CC

InChI

1S/C35H53N2.ClH/c1-9-26(10-2)30-19-17-20-31(27(11-3)12-4)34(30)36-23-24-37(25-36)35-32(28(13-5)14-6)21-18-22-33(35)29(15-7)16-8;/h17-29H,9-16H2,1-8H3;1H/q+1;/p-1

InChI 密鑰

ODQOSTRWDUNLQB-UHFFFAOYSA-M

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相关类别

應用

1,3-Bis(2,6-di(3-pentyl)phenyl)imidazolium chloride is an NHC ligand used in a variety of Pd catalyzed cross-coupling reactions.

其他說明

Pd-PEPPSI-IPent: an active, sterically demanding cross-coupling catalyst and its application in the synthesis of tetra-ortho-substituted biaryls

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Michael G Organ et al.
Angewandte Chemie (International ed. in English), 48(13), 2383-2387 (2009-02-20)
Incredible Bulk: A series of N-heterocyclic carbene catalysts (see picture) were prepared and evaluated in the Suzuki-Miyaura reaction. A variety of sterically encumbered tetra-ortho-substituted biaryl products were formed from unreactive aryl chlorides using the isopentyl-substituted catalyst at temperatures ranging from

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